Chi Yang

发表

Influence of Chromosome 22q11.2 Microdeletion on Postoperative Calcium Level After Cardiac-Correction Surgery

Yibing Ding, Zhengfeng Xu, Zhijuan Ge, 2011, Pediatric Cardiology.

[Prenatal genetic study of fetuses with congenital heart diseases].

Zhengfeng Xu, Yuan Lin, L. Yi, 2009, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

A novel competitive fluorescent multiplex STR polymorphism assay for rapid, reliable and single‐tube screening of 22q11.2 copy‐number aberrations

Yuzhu Peng, D. Qiao, Zhengfeng Xu, 2009, Electrophoresis.

New tetranucleotide STRP markers for detecting the 22q11.2 deletion.

Yali Hu, B. Han, Zhengfeng Xu, 2006, Molecular and cellular probes.

Comparative study of three PCR-based copy number variant approaches, CFMSA, M-PCR, and MLPA, in 22q11.2 deletion syndrome.

Yali Hu, Zhi-yang Shi, Hua Wang, 2009, Genetic testing and molecular biomarkers.

VEGF C−634G polymorphism is associated with protection from isolated ventricular septal defect: case–control and TDT studies

Yali Hu, Jun Xie, D. Qiao, 2007, European Journal of Human Genetics.

Comparative Study of Three PCR-Based Copy Number Variant Approaches , CFMSA , M-PCR , and MLPA , in 22 q 11 . 2 Deletion Syndrome

Yali Hu, Zhi-yang Shi, Hua Wang, 2009 .

FLCN intragenic deletions in Chinese familial primary spontaneous pneumothorax

Lei Cao, Yibing Ding, D. Ma, 2015, American journal of medical genetics. Part A.

[Mutation analysis of the CHD7 gene in patients with congenital heart disease].

Yali Hu, X. Mo, Li Shen, 2008, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Mitochondrial DNA Complex I and I11 Mutations Associated With Leber’s Hereditary Optic Neuropathy

A. Torroni, D. Wallace, M. Lott, 2002 .

22q11.2 microduplication in a family with recurrent fetal congenital heart disease.

Zhengfeng Xu, P. Hu, L. Yi, 2011, European journal of medical genetics.

22 q 11 . 2 microduplication in a family with recurrent fetal congenital heart disease

Zhengfeng Xu, P. Hu, L. Yi, 2011 .

Mutation analysis of the FLCN gene in Chinese patients with sporadic and familial isolated primary spontaneous pneumothorax

D. Qiao, M. Ye, J. Xie, 2008, Clinical genetics.

[Polymorphism of CYP11A1 gene in Chinese patients with polycystic ovarian syndrome].

Zhaolian Wei, Yun-xia Cao, L. Yi, 2010, Zhonghua fu chan ke za zhi.